ライフサイエンスコーパス: agar plate

1 for survival in environments other than the agar plate.

2 ith height variations up to 0.8 mm above the agar plate.

3 e sample as an indication of culturing on an agar plate.

4 ing Bacillus subtilis ATCC 49760 colonies on agar plates.

5 ed in stronger seedling growth inhibition on agar plates.

6 on Luria agar plates and on glucose minimal-agar plates.

7 by a factor of 150 compared to growth on LB agar plates.

8 reening of colonies expressing active p50 on agar plates.

9 and have reduced ability to form colonies on agar plates.

10 at cultures on selective streptococcal blood agar plates.

11 iluted in microtitre plates and spotted onto agar plates.

12 in flagellar swimming motility on semisolid agar plates.

13 y cultured by manual counting of colonies on agar plates.

14 immunoblotting and caseinolytic activity on agar plates.

15 ristic dendritic pattern on semisolid (0.4%) agar plates.

16 ated in duplicate onto selective horse blood agar plates.

17 H. glycines J2 and Caenorhabditis elegans on agar plates.

18 were identified on CAS siderophore detection agar plates.

19 s were exposed to freshly grown H. pylori on agar plates.

20 r bubbles or follow oxygen gradients in soft agar plates.

21 performed directly with colonies from blood agar plates.

22 ng serial aerobic cultivation on tryptic soy agar plates.

23 s lysed, and the lysate was plated onto 7H10 agar plates.

24 henotype (Spp+) on colonies grown on sucrose agar plates.

25 using Arabidopsis thaliana plants growing on agar plates.

26 found arising from the edges of colonies on agar plates.

27 from positive blood cultures using prewarmed agar plates.

28 e for producing nutrient-deficient plants on agar plates.

29 number of bacterial colonies grown on blood agar plates.

30 ion and anchorage-independent growth on soft agar plates.

31 (AST) systems and five selective chromogenic agar plates.

32 tants for a hypohemolytic phenotype on blood agar plates.

33 clusters) were subcultured on 5% sheep blood agar plates.

34 henotype were readily isolated from motility agar plates.

35 onhemolytic Escherichia coli strain on blood agar plates.

36 ed on two different types of VRE chromogenic agar plates.

37 rgans were determined by culture on brucella agar plates.

38 showed enhanced hemolytic activity on blood agar plates.

39 erial four-quadrant streak on 5% sheep blood agar plates.

40 inctive "sectoring" of colonies on selective agar plates.

41 Overexpression of bsrE causes cell lysis on agar plates.

42 d in extensive beta-hemolysis on sheep blood agar plates.

43 during growth in top agar (0.7% agar) or on agar plates (1.2% agar).

44 Air samples were collected on blood agar plates 6 inches from the subject's mouth.

45 After 100P on blood agar plates, 726 genes (33%) of 2192 genes in the S. pne

46 n G27 resulted in decreased motility on soft agar plates, a defect that was complemented by a wild-ty

47 wavy root phenotype when grown vertically on agar plates, a phenotype observed in wild-type plants on

48 orm multicellular patterns as they expand on agar plates, a phenotype that requires a functional copy

49 have the ability to form swarms on motility agar plates after prolonged incubation at 30 degrees C;

50 and an in-house-prepared Mueller-Hinton (MH) agar plate, all incubated for 24 or 48 h; broth microdil

51 um mutant for purple (Pum+ bop+) colonies on agar plates and analyzed for bop mRNA and/or bacteriorho

52 eened for their ability to swarm on motility agar plates and autoagglutinate in liquid cultures; 28 m

53 preparation of DNA from E. coli colonies on agar plates and completion of PCR and melting-curve anal

54 pecies of bacteria were subcultured to blood agar plates and DNA was extracted from the cultures afte

55 tablishing a diffusive gradient in semi-soft agar plates and does not require that the attractant be

56 hange, produced smaller colonies on enriched agar plates and exhibited a 50% decrease in growth rate

57 in protoplasts, in intact seedlings grown on agar plates and in mature plants grown hydroponically.

58 imens after transport to the laboratory onto agar plates and into thioglycolate broth.

59 cal-mucus agar plates but grew well on Luria agar plates and on glucose minimal-agar plates.

60 lagellated counterparts in spreading on soft-agar plates and through medium-filled channels despite h

61 veral limitations, including labor-intensive agar plating and colony selection methods associated wit

62 rate as 0.5% AgNO3, with zero colonies on an agar plate, and about 6 times faster than silver sulfadi

63 in-house-prepared brain heart infusion (BHI) agar plate, and an in-house-prepared Mueller-Hinton (MH)

64 5 outpatients, plated onto a Strep Selective Agar plate, and then tested within 30 min by GASDT.

65 in liquid culture, were unable to spread on agar plates, and lacked flagellar filaments as determine

66 tinely inoculated on colistin-naladixic acid agar plates, and S. aureus was identified by using stand

67 res were subcultured onto blood agar and CNA agar plates, and the plates were reincubated for 24 h.

68 on Module (CDM) for categorizing chromogenic agar plates as negative or "nonnegative" for vancomycin-

69 The fibrin agar plate assay further confirmed the thrombin-mediated

70 e were added were used along with reading of agar plates at both 24 and 48 h.

71 e double-mutant strain was unable to grow on agar plates at O2 tensions of 2.5% or less on N-free med

72 ative, nonspreading organisms on sheep blood agar plates (BAP), having typical gram-negative rod plat

73 were performed from growth on BMHA and blood agar plates (BAP), with and without cefoxitin disk induc

74 g: 100 mul of urine plated onto blood (blood agar plate [BAP]), colistin-nalidixic acid (CNA), and Ma

75 mucus defective), grew poorly on cecal-mucus agar plates but grew well on Luria agar plates and on gl

76 resulting mutants were nonmotile on motility agar plates, but under a light microscope they exhibited

77 of C. perfringens move across the surface of agar plates by a unique type IV pilus (TFP)-mediated soc

78 able fungal culture cases and on double-pour agar plates by using potato dextrose agar in both.

79 C. jejuni harvested from Mueller-Hinton (MH) agar plates, C. jejuni harvested from MH agar plates sup

80 Remel Spectra CRE agar plates can provide useful means for a fast and reli

81 We found that, during agar-plate coculture of these organisms, a signaling eve

82 0.5 McFarland inoculum; and (iii) BHI screen agar plates containing 4 mug/ml vancomycin and 16 g/lite

83 i representing five genera on heart infusion agar plates containing 5% rabbit blood and on brucella a

84 coli, and functional clones were selected on agar plates containing ampicillin.

85 ed clones of M. smegmatis mc2155 screened on agar plates containing chrome azural S, 19 mutants that

86 On agar plates containing glucose, the beneficial effects o

87 4-chloro-3-indolyl-beta-D-galactopyranoside) agar plates containing uracil and uridine after UV irrad

88 Early semiquantitative sputum agar plate culture results can be used to predict sympto

89 enotypes, including loss of motility on soft agar plates, deficiency in siderophore synthesis and iro

90 noculation of multiple scrapes directly onto agar plates (direct method).

91 ocalized Fe supply in horizontally separated agar plates doubled lateral root length without having a

92 ase dependent during growth in liquid and on agar plates during swarmer cell differentiation.

93 ifferent serogroups, were plated on 57 blood agar plates each.

94 n Reynolds cells cultivated on Columbia salt agar plates expressed approximately 100-fold more type 5

95 confirmed by culturing samples overnight on agar plates, followed by a microscopic examination.

96 In contrast, a culture passaged on LB agar plates for 500 generations contained approximately

97 V) agar prior to transfer to Hektoen Enteric agar plates for the recovery of viable Salmonella bacter

98 BEAA and subculture of cocci on sheep blood agar plates for vancomycin disk diffusion and pyrazinami

99 an advantage over conventional direct blood agar plating for the diagnostic confirmation of bartonel

100 onella sp. was isolated on a 5% rabbit blood agar plate from three of six EDTA blood samples.

101 Replicate tests on both types of agar plates generated data to propose zone size limits f

102 in broth, a different result is observed on agar plates: growth of the YidC depletion strain is larg

103 Chloroplasts from plants grown on agar plates had a much higher rate of import than those

104 In the assay, bacterial lawns were grown on agar plates, harvested with phosphate-buffered saline, b

105 st research on growing bacterial colonies on agar plates has concerned the effect of genetic or morph

106 direct finger impressions on inhibitory mold agar plates, (ii) bag washes in brain heart infusion bro

107 st area, and assistant's chest area on blood agar plates in all three groups.

108 , but instead permitted the cells to grow on agar plates in the absence of an external carbon source.

109 t detection of residual agar from culture on agar plates in the presence of bacterial spores with a l

110 nosa exhibits swarming motility on 0.5 to 1% agar plates in the presence of specific carbon and nitro

111 th mutants were completely nonmotile on soft agar plates, in minimal broth, and in tomato plants.

112 Other agar plates included Sabouraud's, buffered charcoal-yeas

113 were tested using Mueller-Hinton sheep blood agar plates incubated for 20 to 24 h in 5% CO2; they wer

114 se obtained with conventional anaerobe blood agar plates incubated in an anaerobe chamber.

115 Head-to-head competition assays on agar plates indicate that two-dimensional constraint on

116 to densities that are >/= 10(9) CFU/ml or on agar plates is described.

117 When Legionella pneumophila grows on agar plates, it secretes a surfactant that promotes flag

118 e M. tuberculosis mshD mutant grew poorly on agar plates lacking catalase and oleic acid and in low-p

119 ssor tRNA yielded transformants that grow on agar plates lacking uracil.

120 fore autoclaving the agar, or Mueller-Hinton agar plates may be flooded with a glucose-methylene blue

121 e agar before autoclaving, or Mueller-Hinton agar plates may be flooded with a glucose-methylene blue

122 erature before plating, 51% used Campy blood agar plate medium, 52% read plates at <72 hours of incub

123 compared to those obtained by a conventional agar plate method for a total of 805 synovial fluid spec

124 TEC Peds Plus/F bottle over the conventional agar plate method for the detection of clinically signif

125 ontaminants [P = 0.006]) than culture by the agar plate method.

126 Compared to the conventional agar plating method, the assay was rapid (1.5 h) and sho

127 in heart infusion-6-micrograms/ml vancomycin agar plates obtained from five commercial sources (B-D M

128 Agar plates of fungi present a complex topography due to

129 d included direct inoculation of a MacConkey agar plate on which a 10-mug meropenem disk was placed a

130 on Broth or on Muller-Hinton-based chocolate agar plates or genetic mutation of Ft was found to compr

131 or B anthracis collected on open sheep blood agar plates (P<.001) and personal air monitors (P =.01)

132 Prepared MH-GMB agar plates provide acceptable performance for disk diff

133 d with results obtained with the double-pour agar plates (rated as "good"), fungal growth and identif

134 On agar plates, red colonies are simply visualized in ambie

135 Furthermore, extended passage on blood agar plates reduces the expression of genes associated w

136 cts in the chemotaxis signaling pathway, the agar plates remain dry and the cells' flagella are short

137 nificantly greater inhibition by H(2)O(2) on agar plates (reversed by complementation), 30% less adhe

138 agar was compared to culture on sheep blood agar plate (SBAP) and AccuProbe detection of group B str

139 However, in various types of motility agar plates, sirA was able to activate a sopB fusion by

140 ot confer a hard colony phenotype on sucrose agar plates, suggesting that the type of glucan product

141 MH) agar plates, C. jejuni harvested from MH agar plates supplemented with DOC secreted the Cia prote

142 We compared the abilities of media from agar plates surrounding swarming and nonswarming cells o

143 lized microtubes was assessed by qualitative agar plate test using Micrococcus luteus as substrate sh

144 (measured edge to edge) on a Mueller-Hinton agar plate that had been inoculated with an S. aureus is

145 Modified Leeds Acinetobacter medium (mLAM) agar plates that contained vancomycin and either aztreon

146 was plated directly onto a gentamicin blood agar plate; the other was placed in STGG.

147 em greatly impaired in motility on semisolid agar plates; this defect can be corrected by the introdu

148 We compared the Remel Spectra CRE agar plate to CDC standard methodology for the isolation

149 nsferred through a succession of nonnutrient agar plates to eliminate fungal and other contaminants.

150 sing a system of polyethylene glycol-infused agar plates to impose a constant low-water-potential str

151 s for the use of polyethylene glycol-infused agar plates to impose low water potential stress, assay

152 chment broths onto 150-mm sorbitol-MacConkey agar plates to which cefixime and tellurite were added w

153 rabidopsis thaliana) seedlings were grown on agar plates under different salt stress conditions.

154 uxArray 1.0 reporter strains to membranes on agar plates was used for simultaneous reporter gene assa

155 ant inbred strains assayed on the surface of agar plates, we found QTL for survival, early fertility,

156 : when roots growing along the surface of an agar plate were gravistimulated, there was often an upwa

157 Agar plates were evaluated for the presence of pink colo

158 The blood agar plates were incubated at 37 degrees C for 48 hours,

159 imens; ESP II was positive first for 33, and agar plates were positive first for 7.

160 MH-GMB agar plates were prepared as described in National Commi

161 Agar plates were shown to contain a small amount of gala

162 mucoid colony phenotype when grown on blood agar plates were temporally associated with the higher i

163 ies of a 6PGDH mutant library growing on the agar plates were treated by heat to minimize the backgro

164 ch showed good growth and DNA replication on agar plates, were irradiated at (DNA-effective) UV-B flu

165 was used for Mimivirus isolation, which used agar plates where the growth of giant viruses is reveale

166 ciated with the use of a primary tryptic soy agar plate with 5% sheep blood (BAP) and a 3-ml tube of

167 of meropenem and subcultured to a MacConkey agar plate with a 10-mug meropenem disk) and for sequenc

168 Replicate tests on both types of agar plates with 1- micro g voriconazole disks generated

169 s containing 5% rabbit blood and on brucella agar plates with and without sheep blood under aerobic,

170 f metabolites in tissues, cell cultures, and agar plates with cellular resolution, but it is hampered

171 When D. discoideum is plated on nutrient agar plates with different P. aeruginosa strains, the ba

172 Samples were cultured on blood agar plates with gentamicin and screened for alpha-hemol

173 Cells from dense colonies grown on agar plates with LB broth or synthetic (Neidhardt) mediu

174 tants were tested for the ability to grow on agar plates with mouse cecal mucus as the sole source of

175 rs with an enlarged base after transfer from agar plates with normal medium to plates with 6% Glc.

176 When grown in agar plates with reduced iron concentration, triple bhlh

177 detected from hyphae of the fungus grown on agar plates, without the need for any organic extraction